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Evaluation of Galactomannan Testing, the Aspergillus-Specific Lateral-Flow Device Test and Levels of Cytokines in Bronchoalveolar Lavage Fluid for Diagnosis of Chronic Pulmonary Aspergillosis
被引:29
|作者:
Salzer, Helmut J. F.
[1
,2
]
Prattes, Juergen
[2
,3
]
Flick, Holger
[2
,4
]
Reimann, Maja
[1
,2
]
Heyckendorf, Jan
[1
,2
]
Kalsdorf, Barbara
[1
,2
]
Obersteiner, Sabrina
[2
,3
,5
]
Gaede, Karoline, I
[2
,6
,7
]
Herzmann, Christian
[2
,8
,9
]
Johnson, Gemma L.
[2
,10
]
Lange, Christoph
[1
,2
,11
,12
]
Hoenigl, Martin
[2
,3
,4
,13
]
机构:
[1] Res Ctr Borstel, Div Clin Infect Dis, Borstel, Germany
[2] German Ctr Infect Res DZIF, Partner Site Hamburg Lubeck Borstel, Borstel, Germany
[3] Med Univ Graz, Sect Infect Dis & Trop Med, Graz, Austria
[4] Med Univ Graz, Dept Internal Med, Div Pulmonol, Graz, Austria
[5] CBmed Ctr Biomarker Res Med, Graz, Austria
[6] Leibniz Ctr Med & Biosci, Res Ctr Borstel, BioMaterialBank North, Borstel, Germany
[7] German Ctr Lung Res, Airway Res Ctr North, Borstel, Germany
[8] Res Ctr Borstel, Ctr Clin Studies, Borstel, Germany
[9] German Ctr Infect Res, Clin Trials Unit, Borstel, Germany
[10] OLM Diagnost, Newcastle Upon Tyne, Tyne & Wear, England
[11] Univ Lubeck, Int Hlth Infect Dis, Lubeck, Germany
[12] Karolinska Inst, Dept Med, Stockholm, Sweden
[13] Univ Calif San Diego, Dept Med, Div Infect Dis, San Diego, CA 92103 USA
来源:
FRONTIERS IN MICROBIOLOGY
|
2018年
/
9卷
关键词:
chronic pulmonary aspergillosis;
bronchoalveolar lavage;
galactomannan;
lateral-flow device;
cytokines;
INVASIVE ASPERGILLOSIS;
SERUM;
GUIDELINES;
MANAGEMENT;
DISEASES;
ANTIGEN;
ASSAYS;
D O I:
10.3389/fmicb.2018.02223
中图分类号:
Q93 [微生物学];
学科分类号:
071005 ;
100705 ;
摘要:
Background: Diagnosis of chronic pulmonary aspergillosis (CPA) is challenging. Symptoms are unspecific or missing, radiological findings are variable and proof of mycological evidence is limited by the accuracy of diagnostic tests. The goal of this study was to investigate diagnostic performance of galactomannan (GM), the newly formatted Aspergillus-specific lateral-flow-device test (LFD), and a number of cytokines in bronchoalveolar lavage fluid (BALF) samples obtained from patients with CPA, patients with respiratory disorders without CPA and healthy individuals. Methods: Patients with CPA (n = 27) and controls (n = 27 with underlying respiratory diseases but without CPA, and n = 27 healthy volunteers) were recruited at the Medical University of Graz, Austria and the Research Center Borstel, Germany between 2010 and 2018. GM, LFD and cytokine testing was performed retrospectively at the Research Center Borstel. Results: Sensitivity and specificity of GM testing from BALE with a cut off level of >= 0.5 optical density index (ODI) was 41 and 100% and 30 and 100% with a cut off level of >= 1.0 ODI. ROC curve analysis showed an AUC 0.718 (95% CI 0.581-0.855) for GM for differentiating CPA patients to patients with other respiratory diseases without CPA. The LFD resulted positive in only three patients with CPA (7%) and was highly specific. CPA patients did not differ significantly in the BALF cytokine profile compared to patients with respiratory disorders without CPA, but showed significant higher values for IFN-gamma, IL-1 b, IL-6, IL-8, and TNF-alpha compared to healthy individuals. Conclusion: Both GM and LFD showed insufficient performance for diagnosing CPA, with sensitivities of BALF GM below 50%, and sensitivity of the LFD below 10%. The high specificities may, however, result in a high positive predictive value and thereby help to identify semi-invasive or invasive disease.
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